A triflate and alkynyl protected Ag43 nanocluster with a passivated surface

A trifluoromethanesulfonate (OTf) and tert-butylacetylene (tBuC 
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Created by potrace 1.16, written by Peter Selinger 2001-2019
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 C−) co-protected silver nanocluster (NC), Ag43(tBuCC)24(CF3SO3)8 (Ag43), was synthesized and characterized. Single crystal X-ray diffraction analysis revealed its total structure. 43 Ag atoms are arranged into a three-concentric-shell Ag@Ag12@Ag30 structure. Both OTf and tBuCC− ligands bonded with Ag atoms in a μ3 mode. The application of Ag43 as a catalyst for the reaction of silane with alcohol or H2O indicated that the surface ligands had a profound passivation effect, which significantly influenced the reactivity and selectivity.


Introduction
Metal NCs have attracted a great amount of attention during the past decades not only for their aesthetic values but also for their potential applications in self-assembly, surface plasmon resonance (SPR), bio-markers, (electro)catalysis, etc. [1][2][3][4][5][6] Fundamentally relating their structures with their properties, however, has encountered huge challenges. 7 One obstacle is the difficulty in precisely characterizing the structures of NCs. To this end, many practical methodologies have been brought forward. Among them, single-crystal crystallography has special advantages in determining the total structures of NCs. 8 Aiming to resolve the target's structure at atomic level, this methodology has found incomparable advantage in revealing the organicmetal interfacial structure of NCs. For example, the unprecedented "staple" bonding motif of thiolate of Au 102 NC was rstly revealed by this method. 9,10 There has since been a boom in the study of the potential applications of the atomically precise NCs, especially catalysis. 11 The promoting effect of the surface ligands have been repeatedly observed in different types of reactions. 12,13 However, to obtain the single crystals of NCs, the strong interaction between the NCs and ligands is usually necessary for stabilizing the NCs. Thus, the surface catalytically active sites might be blocked by the organic ligands. However, the researches addressing this issue of Ag NCs seem rare.
On the other side, a large number of thiolate and(or) phosphine protected Au or Ag NCs have been synthesized so far, such as Au 25 22 and many others. 23 Beyond the conventional ligands, alkynes are drawing fast-increasing attentions, thanks to the exible bonding modes of alkynes with metals. [24][25][26][27][28] In recent years, there have been a considerable amount of NCs containing anions in their structures. Most of them, however, function as templates or counterions. [29][30][31][32] Ag NCs or complexes featuring direct Ag-O bonding are mostly those with Ag(I) species. 33 Examples of Ag(0) NCs protected by inorganic oxo anions are rare. Sun etc. recently reported a Ag(0) NC co-protected by CrO 4 2À and t BuC^C À , [Ag 48 (C^C t Bu) 20 (CrO 4 ) 7 ]. 34 Herein, we report the rst example of a Ag(0) NC co-protected by triate (OTf) and tert-butylacetylene ( t BuC^C À ), namely, Ag 43 ( t BuC^C) 24 (CF 3 SO 3 ) 8 (denoted as Ag 43 ). The detailed structure of Ag 43 is analyzed and discussed. Significantly, we have found a strong passivation effect in the reaction of silanes with alcohol or H 2 O catalyzed by Ag 43 . This effect not only sharply decreased the reaction rate, but also exerted a direct inuence on the reaction selectivity.

Results and discussion
Ag 43 was synthesized by introducing a reducing agent, NaBH 4 into an ethanol solution of AgSO 3 CF 3 , tert-butylacetylene ( t BuC^C À ), 1,4-bis-(diphenylphosphino)butane (dppb), and triethylamine (Et 3 N). The reaction was aged for 24 hours during which the colour gradually changed from pale-yellow to dark green. A block-shaped single crystal was obtained by slowly diffusing a mixed solvent of hexane and ether into the mother solution (ESI, Fig. S1 †). Ag 43 crystallizes in I2/m space group and its overall structure is shown in Fig. 1 and S2. † It consists of 43 silver atoms, 24 t BuC^C À and 8 OTf ligands. The Ag atoms are arranged into a three-shell Russian doll structure, Ag@Ag 12 @-Ag 30 (Fig. 1b). The Ag@Ag 12 shells make up an icosahedron with a dodeca-coordinated Ag atom at the center (Fig. 1c). Bearing a Ag atom bonding with only Ag atoms endows Ag 43 with partial Ag(0) character. The rest 30 Ag atoms of the outermost shell form 12 pentagons and 20 triangles. The two regular polygons are connected through edge-sharing, which makes each pentagon be enclosed by ve triangles and each triangle by three pentagons. Geometrically, such an arrangement forms an icosidodecahedron, an Archimedean solid (Fig. 1d). The outermost shell is closely related with the ligands' distribution (see below). The average Ag-Ag bond length between the central Ag to Ag 12 shell is 2.858 A, while the value is 3.1 A between Ag 12 and Ag 30 shells. Both are less than the sum of the van der Waals radii of two Ag atoms (3.44 A), indicating argyrophilic interactions between the shells. As mentioned, the distribution of peripheral ligands is dependent on the arrangement of silver atoms, especially the Ag 30 shell (Fig. 2a). There are 24 t BuC^C À ligands which can be equally divided into two groups. Each of the rst half penetrates one of the twelve pentagons of Ag 30 shell and bonded to Ag 12 shell through s bond. Each of the twelve t BuC^C À also bonds with the pentagon through p bonds (Fig. 2a). The rest 12 t BuC^C À ligands along with 8 OTf ligands, which amount to 20, coordinated with the 20 triangles of the Ag 30 shell respectively. It is noteworthy that every t BuC^C À and OTf has the similar m 3 coordination mode (Fig. 2b and c). It is also worth noting that although OTf bonding with Ag atoms are commonly seen in Ag(I) complexes or clusters, especially those with low nuclearity, 35,36 Ag(0) NC protected by OTf has barely been reported. The bond length of the Ag-O bond is 2.415 A, which is within the common range typical Ag-O bonds. 37,38 We investigated the optical properties of Ag 43 in CH 2 Cl 2 (Fig. 3). As illustrated in Fig. 3a, the UV-vis absorption spectrum of Ag 43 shows two absorption features: one major peak at 434 nm and a shoulder at 620 nm. FT-IR spectra of Ag 43 , t BuC^C À and the precursor AgSO 3 CF 3 are shown in Fig. 3b. The stretching of^C-H at 3272 cm À1 is no longer present in Ag 43 , indicating the bonding of t BuC^C À with Ag. 39 The characteristic peaks of SO 3 CF 3 À ranging from 1000 to 1500 cm À1 , on the other hand, are still prominent in the spectrum of Ag 43 . These information further conrmed both ligands are present on Ag 43 . The possible inuence of the Ag 43 surface ligands on catalysis was evaluated in the reaction of a sterically demanding substrate dimethylphenylsilane (denoted as silane) with H 2 O or 1-butanol (Scheme 1). 40,41 As a benchmark, polyvinylpyrrolidone (PVP) stabilized Ag nanoparticles (Ag/PVP) were also fabricated following a reported procedure. 42 The results are summarized in Fig. 1 (a) The overall structure of Ag 43 ( t BuC^C) 24 4. We can see that for either H 2 O or alcohol as substrate, the reaction catalyzed by Ag 43 always showed signicantly lower reactivity than Ag/PVP, although the amount of Ag as well as the other reaction conditions were kept the same (Fig. 4a and c). Despite the small size of Ag 43 (less than 1 nm), the surface ligands still exerted a direct impact on limiting the contact of substrate with Ag. This also inuenced the product distribution. For Ag/PVP, full selectivity towards the target was always achieved. Ag 43 , however, afforded a signicant amount of 1,3diphenyl-1,1,3,3-tetramethyldisiloxane (denoted as disiloxane). As the reaction proceeded, the byproduct kept accumulating. For example, in hydrolysis reaction catalyzed by Ag 43 , when half the silane was consumed, the byproduct disiloxane accounted for 54% of the total product (Fig. 4b). The situation was similar in dehydrogenative coupling with 1-butanol (Fig. 4d). Not only the reaction rate was slower for Ag 43 , but disiloxane was also found as a major part of the products. Ag was fairly stable under such reaction condition. The light absorption Ag 43 aer reaction has similar features (Fig. S3 †). Generally, the rate-limiting step of this reaction is the activation of alcohol. Thus, given the full occupation of the surface Ag site, this step might be inhibited, which gave silane more chance to react with each other. The exact mechanism, however, still requires further thorough investigation.

Conclusions
In conclusion, a triate and tert-butylacetylene protected Ag 43 is synthesized and characterized. For the rst time the triate is shown to function as an effective surface ligand for Ag (0) nanocluster. It bonds with Ag atoms in m 3 mode. Although Ag 43 has a very small size, its catalytic ability is signicantly worse than the PVP protected Ag nanoparticles. The surface ligands of Ag 43 showed strong passivation effect for the reaction of silane with H 2 O or butanol. Such an effect also sharply decreased the selectivity towards the desired target, yielding a signicant percentage of disiloxane as byproduct.

Conflicts of interest
There are no conicts to declare.